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Hydrochloric Acid → 7-Bromo-benzo[d]isothiazol-5-ylamine

HRID 389470
ノート
印刷プレビュー

反応式

HRID 389470 の反応式
[Br:1][C:2]1[C:10]2[S:9][N:8]=[CH:7][C:6]=2[CH:5]=[C:4]([N+:11]([O-])=O)[CH:3]=1.Cl>C(O)C.[Fe]>[Br:1][C:2]1[C:10]2[S:9][N:8]=[CH:7][C:6]=2[CH:5]=[C:4]([NH2:11])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 313Hydrochloric AcidHCID 66759851HCID 66759851、化合物

生成物 1

HCID 667606927-Bromo-benzo[d]isothiazol-5-ylamine収率 56%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 702Ethanol溶媒

実験手順

A mixture of 7-bromo-5-nitro-benzo[d]isothiazole (1.0 g, 3.9 mmol) and iron powder (1.0 g, 19 mmol) in ethanol (40 mL) was heated to reflux with vigorous stirring. An aqueous 0.1 N hydrochloric acid (10 mL, 1 mmol) solution was added and the reaction continued until TLC showed no starting material. The reaction mixture was cooled to RT and filtered. The filtrate was concentrated and aqueous sodium carbonate was added to the residue until it became basic. This mixture was filtered through Celite, washing with ethyl acetate. The organic layer was separated, washed with water, dried over anhydrous sodium sulfate and concentrated to give 500 mg (56%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 8.8 (s, 1H), 7.2 (s, 1H), 7.1 (s, 1H), 3.82 (br. s, 2H).

後処理

  1. temperaturewas heated
  2. temperatureto reflux with vigorous stirring
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated
  5. additionaqueous sodium carbonate was added to the residue until it
  6. filtrationThis mixture was filtered through Celite
  7. washwashing with ethyl acetate
  8. customThe organic layer was separated
  9. washwashed with water
  10. dry with materialdried over anhydrous sodium sulfate
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-6d655562fa0d41e1b89203cf9d38a70e
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08378104B2

反応ノート

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